sop for drying of silica gel 1.0 OBJECTIVE: To lay down a procedure for Drying of Silica Gel in Quality Control Lab. 2.0 SCOPE: This SOP is applicable of procedure for Drying of Silica Gel in Quality Control department 3.0 RESPONSIBILITY: Executive/Officer QC/designee. 4.0 ACCOUNTABILITY: Head- Quality Control 5.0 PROCEDURE 5.1 Silica … Read more
sop for operation of infrared moisture balance 1.0 OBJECTIVE 1.1 To describe a procedure for operating, & calibration of IR Moisture Balance. 2.0 SCOPE 2.1 This procedure is applicable for operating, & calibration of IR Moisture Balance to the Quality control department 3.0 RESPONSIBILITY 3.1 Officer/Executive – QC 4.0 ACCOUNTABILITY 4.1 Head … Read more
sop for preparation of mobile phase 1.0 OBJECTIVE: To lay down a procedure for the Procedure for preparation of mobile phase in Quality Control department during analysis. 2.0 SCOPE: This SOP procedure is applicable for Quality Control Department 3.0 RESPONSIBILITY: Officer / Executive – QC 4.0 ACCOUNTABILITY: Head – QC 5.0 PROCEDURE: Read … Read more
sop for treated RO water STORAGE REQUIREMENTS Store at room temperature in a well closed stainless steel or glass container. a) Analysis samples drawn for chemical analysis within 24 hours after sampling. b) Analysis samples drawn for microbiological analysis within 8 hours after sampling. Refrigerate the samples (between 2°C to 8°C) until testing … Read more
sop for Preparation and Issuance of Analysis protocol standard 1.0 OBJECTIVE: To lay down a procedure for the “Preparation and Issuance of Analysis protocol” for Raw material, Packing material, In-process sample, Stability Product and Finished Product. 2.0 SCOPE: This SOP is applicable for “Preparation and Issuance of Analysis protocol” for Raw material, … Read more
sop of placebo and impurity stock solutions 1.0. OBJECTIVE: To lay down a procedure for Handling of Placebo And Impurity Stock Solutions. Placebo: A placebo is an inactive drug composition or composition of drug without any Active Pharmaceuticals Ingredient. Impurity: The unwanted chemicals that remain with active pharmaceuticals ingredients, or develop during formulation or … Read more
sop for disposal of residual sample 1.0. OBJECTIVE : 1.1 To lay down a procedure for disposal of Residual sample of Quality Control Department. 2.0. SCOPE: 2.1 This procedure is applicable for disposal of Residual sample of Quality Control Department . 3.0. RESPONSIBILITY : 3.1 Officer/ Executive shall be responsible for disposal of … Read more
sop for handling of pharmacopoeial changes 1.0 OBJECTIVE: To lay down a procedure for “Handling of Pharmacopoeial Changes”. 2.0 SCOPE: This SOP is applicable of procedure for “Handling of Pharmacopoeial Changes” in quality control department 3.0 RESPONSIBILITY: Executive QC/Officer QC 4.0 ACCOUNTABILITY: Head- Quality Control 5.0 PROCEDURE 5.1 Procurement of Pharmacopoeial Publications: Pharmacopoeial publications include … Read more
sop for procedure for operation of ultrasonic cleaner 1.0 OBJECTIVE procedure for operation of ultrasonic cleaner 1.1 To describe a procedure for Ultrasonic Cleaner. 2.0 SCOPE 2.1 This procedure is applicable to the Quality control department of Quality control 3.0 RESPONSIBILITY 3.1 Officer /Executive – QC 4.0 ACCOUNTABILITY 4.1 Head –QC 5.0 PROCEDURE … Read more
difference between UPLC and HPLC UPLC full form Ultra Performance Liquid Chromatography. UPLC instrument is modern and more power full technology standard HPLC stage because of its force for expanding test throughput, chromatographic sensitivity effciencyand decreasing run time. UPLC (Ultra Performance Liquid Chromatography) instrument it is pressure up to 15000 psi HPLC full … Read more